ALS5/SPG11/ KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease (2016)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awv320
PubMed Identifier: 26556829
Publication URI: http://europepmc.org/abstract/MED/26556829
Type: Journal Article/Review
Parent Publication: Brain
Issue: 1
ISSN: 0006-8950